Benign familial mesial temporal lobe epilepsy   770405003

SNOMED CT code


SNOMED code770405003
nameBenign familial mesial temporal lobe epilepsy
statusactive
date introduced2019-01-31
fully specified name(s)Benign familial mesial temporal lobe epilepsy (disorder)
synonyms
  • Benign familial mesial temporal lobe epilepsy
  • Benign FMTLE (familial mesial temporal lobe epilepsy)
attributes - group1
Finding siteTemporal lobe structure   78277001
parents
  • Autosomal dominant hereditary disorder   11164009
  • Temporal lobe epilepsy   193000002
  • Hereditary disorder of nervous system   363235000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Benign familial mesial temporal lobe epilepsy   770405003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of head and neck region   118254002
      Head finding   406122000
        Finding of head region   298364001
          Temporal lobe epilepsy   193000002
            Benign familial mesial temporal lobe epilepsy   770405003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of nervous system   118940003
          Hereditary disorder of nervous system   363235000
            Benign familial mesial temporal lobe epilepsy   770405003

ancestors
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